Anthony Antonellis

Biochemistry, Genetics and Molecular BiologyNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 11 papers. Top paper: “Loss‐of‐Function CARS1 Variants in a Patient With Microcephaly, Developmental Delay, and a Brittle Hair Phenotype”.

Loss‐of‐Function CARS1 Variants in a Patient With Microcephaly, Developmental Delay, and a Brittle Hair Phenotype

Molecular Genetics & Genomic Medicine(2025)10.1002/mgg3.70078

N/A

0.165DataRank · unranked

2 citations

Molly E. Kuo, Desirée E.C. Smith, Marisa I. Mendes, Gajja S. Salamons, Marek Nemčovič +5 more

GARS‐related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61544

N/A

0DataRank · unranked

28 citations

Rajarshi Ghosh, Molly E. Kuo, William Hong, Jaehyung Lim, Saunder Bernes +14 more

Translatomic analysis of regenerating and degenerating spinal motor neurons in injury and ALS

iScience(2021)10.1016/j.isci.2021.102700

N/A

0DataRank · unranked

27 citations

Wesley M. Stansberry, Allison M. Milen, Rachel E. Ives, Elizabeth A. Fogarty, Anthony Antonellis +2 more

A missense, loss-of-functionYARS1variant in a patient with proximal-predominant motor neuropathy

Molecular Case Studies(2022)10.1101/mcs.a006246

N/A

0DataRank · unranked

3 citations

Alayne P. Meyer, Stephanie M. Laureano Figueroa, Anthony Antonellis, Megan E. Forrest

A humanized yeast model reveals dominant-negative properties of neuropathy-associated alanyl-tRNA synthetase mutations

Human Molecular Genetics(2023)10.1093/hmg/ddad054

N/A

0DataRank · unranked

13 citations

Sheila Marte, T.J. Smith, Shawna Feely, Marina Kennerson, Garth A. Nicholson +4 more

Dominant NARS1 mutations causing axonal Charcot–Marie–Tooth disease expand NARS1-associated diseases

Brain Communications(2024)10.1093/braincomms/fcae070

N/A

0DataRank · unranked

18 citations

Sheila Marte, Jiaxin C Li, Willem De Ridder, Jessie Z Chen, Abigail L. D. Tadenev +12 more

A model organism pipeline provides insight into the clinical heterogeneity of TARS1 loss-of-function variants

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100324

N/A

0DataRank · unranked

0 citations

Allison R. Cale, Jennifer A. Pierluissi, Kira E. Jonatzke, Young N. Park, Guy M. Lenk +7 more

Recessive, pathogenic AARS1 variants display variable loss-of-function and dominant-negative effects

Disease Models & Mechanisms(2025)10.1242/dmm.052006

N/A

0DataRank · unranked

2 citations

Kira E. Jonatzke, M.E. Parish, Anthony Antonellis, Molly E. Kuo

Atypical Presentation of IARS1‐Related Disorder: Expanding the Phenotype and Genotype

JIMD Reports(2025)10.1002/jmd2.70020

N/A

0DataRank · unranked

1 citations

Kira E. Jonatzke, Benjamin T. Hyde, Lance W. Peterson, Mai He, Robert C. McKinstry +3 more

Contributors

Genomic and Personalized Medicine(2009)10.1016/b978-0-12-369420-1.00122-0

N/A

0DataRank · unranked

0 citations

Matthew L. Anderson, Felicita Andreotti, Brian H. Annex, Anthony Antonellis, Dmitri Artemov +272 more

Asparaginyl-tRNA synthetase (NARS1) variants implicated in dominant neurological phenotypes display dominant-negative properties

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100519

N/A

0DataRank · unranked

0 citations

Keyana Blake, Brendan L M Sutton, Marina Konyukh, Stephan Züchner, Tanya Stojkovic +3 more